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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275062Generated: November 3, 2026

HCID 66834104, compound → 2-[1-(6-Cyano-1-methanesulfonyl-1H-indol-2-yl)-1-methylethyl]-4-methoxy-benzoic acid methyl ester

https://huagongshe.com/reaction/2275062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66834104HCID 66834104—
Reactant2-(1,1-Dimethylprop-2-ynyl)-4-methoxy-benzoic acid methyl esterHCID 86663815—
CatalystCopper iodideHCID 83717—
SolventDimethylformamideHCID 6228—
Product2-[1-(6-Cyano-1-methanesulfonyl-1H-indol-2-yl)-1-methylethyl]-4-methoxy-benzoic acid methyl esterHCID 6683428262%

Reaction Conditions

Temperature90 °C

Reaction Steps

To the DMF (2 ml) solution of 2-(1,1-dimethylprop-2-ynyl)-4-methoxy-benzoic acid methyl ester (Compound AA3, 134 mg, 0.577 mmol) and N-(2-bromo-5-cyanophenyl)methanesulfonamide (Compound AA5, 167 mg, 1.05 eq.), copper iodide (9 mg, 0.08 eq.) and TEA (129 μl, 1.6 eq.) were added, degassed and flushed with nitrogen gas, added with dichlorobis(triphenylphosphine) palladium (20 mg, 0.05 eq.), and then degassed and flushed again with nitrogen gas. After stirring for 2 hr at 90° C., the reaction solution was added with water, extracted with ethyl acetate. The organic layer was washed with an brine and dried over magnesium sulfate. The drying agent was removed by filtration and the residues obtained after concentration under reduced pressure were purified by silica gel column chromatography (ethyl acetate/hexane) to obtain the title compound (white solid, 152 mg, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126931B2
Source datasetuspto-grants-2015_09
ORD IDord-40d70ae733db4a5db4294d8709880f77
Source noteuspto-grants-2015_09